Ticagrelor monotherapy after PCI in patients with concomitant diabetes mellitus and chronic kidney disease: TWILIGHT DM-CKD.


Journal

European heart journal. Cardiovascular pharmacotherapy
ISSN: 2055-6845
Titre abrégé: Eur Heart J Cardiovasc Pharmacother
Pays: England
ID NLM: 101669491

Informations de publication

Date de publication:
29 Sep 2022
Historique:
received: 07 01 2022
revised: 17 02 2022
pubmed: 25 3 2022
medline: 1 10 2022
entrez: 24 3 2022
Statut: ppublish

Résumé

We aimed to evaluate the treatment effects of ticagrelor monotherapy in the very high risk cohort of patients with concomitant diabetes mellitus (DM) and chronic kidney disease (CKD) undergoing percutaneous coronary intervention (PCI). In the TWILIGHT (Ticagrelor with Aspirin or Alone in High-Risk Patients after Coronary Intervention) trial, after 3-month dual antiplatelet therapy with ticagrelor and aspirin post-PCI, event-free patients were randomized to either aspirin or placebo in addition to ticagrelor for 12 months. Those with available information on DM and CKD status were included in this subanalysis and were stratified by the presence or absence of either condition: 3391 (54.1%) had neither DM nor CKD (DM-/CKD-), 1822 (29.0%) had DM only (DM+/CKD-), 561 (8.9%) had CKD only (DM-/CKD+), and 8.0% had both DM and CKD (DM+/CKD+). The incidence of the primary endpoint of Bleeding Academic Research Consortium (BARC) type 2, 3, or 5 bleeding did not differ according to DM/CKD status (P-trend = 0.13), but there was a significant increase in BARC 3 or 5 bleeding (P-trend < 0.001) as well as the key secondary endpoint of death, myocardial infarction, or stroke (P-trend < 0.001). Ticagrelor plus placebo reduced bleeding events compared with ticagrelor plus aspirin across all four groups, including DM+/CKD+ patients with respect to BARC 2-5 [4.5% vs. 8.7%; hazard ratio (HR) 0.49, 95% confidence interval (CI) 0.24-1.01] as well as BARC 3-5 (0.8% vs. 5.3%; HR 0.15, 95% CI 0.03-0.53) bleeding, with no evidence of heterogeneity. The risk of death, myocardial infarction, or stroke was similar between treatment arms across all groups. Irrespective of the presence of DM, CKD, and their combination, ticagrelor monotherapy reduced the risk of bleeding without a significant increase in ischaemic events compared with ticagrelor plus aspirin.

Identifiants

pubmed: 35325085
pii: 6552954
doi: 10.1093/ehjcvp/pvac016
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Ticagrelor GLH0314RVC
Aspirin R16CO5Y76E

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

707-716

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Payam Dehghani (P)

Department of Cardiology, Prairie Vascular Research, Regina, Saskatchewan, Canada.

Davide Cao (D)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele-Milan, Italy.

Usman Baber (U)

Department of Cardiology, the University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

Johny Nicolas (J)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

Samantha Sartori (S)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

Carlo A Pivato (CA)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.
Cardio Center, IRCCS Humanitas Research Hospital, Rozzano-Milan, Italy.

Zhongjie Zhang (Z)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

George Dangas (G)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

Dominick J Angiolillo (DJ)

Division of Cardiology, University of Florida College of Medicine, Jacksonville, FL, USA.

Carlo Briguori (C)

Department of Cardiology, Mediterranea Cardiocentro, Naples, Italy.

David J Cohen (DJ)

Cardiovascular Research Foundation, New York, NY, USA.
Department of Cardiology, St. Francis Hospital, Roslyn, NY, USA.

Timothy Collier (T)

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

Dariusz Dudek (D)

Institute of Cardiology, Jagiellonian University Medical College, Krakow, Poland.

Michael Gibson (M)

Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Robert Gil (R)

Center of Postgraduate Medical Education, Central Clinical Hospital of the Ministry of Interior and Administration, Warsaw, Poland.

Kurt Huber (K)

3rd Department of Medicine, Cardiology and Intensive Care Medicine, Wilhelminen Hospital, and Medical Faculty, Sigmund Freud University, Vienna, Austria.

Upendra Kaul (U)

Heart Centre, Batra Hospital and Medical Research Centre, New Delhi, India.

Ran Kornowski (R)

Department of Cardiology, Rabin Medical Center, Petach Tikva, Israel.

Mitchell W Krucoff (MW)

Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Vijay Kunadian (V)

Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University and Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Shamir Mehta (S)

Population Health Research Institute, Hamilton Health Sciences, Hamilton, ON, Canada.

David J Moliterno (DJ)

Division of Cardiovascular Medicine, Gill Heart Institute, University of Kentucky, Lexington, KY, USA.

E Magnus Ohman (EM)

Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Javier Escaned (J)

Department of Cardiology, Hospital Clínico San Carlos IDISCC, Complutense University of Madrid, Madrid, Spain.

Gennaro Sardella (G)

Department of Cardiology, Policlinico Umberto I University, Roma, Italy.

Samin K Sharma (SK)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

Richard Shlofmitz (R)

Department of Cardiology, St. Francis Hospital, Roslyn, NY, USA.

Giora Weisz (G)

Division of Cardiology, NewYork Presbyterian Hospital, Columbia University Medical Center, New York, NY, USA.

Bernhard Witzenbichler (B)

Department of Cardiology and Pneumology, Helios Amper-Klinikum, Dachau, Germany.

Stuart Pocock (S)

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

Roxana Mehran (R)

Center for Interventional Cardiovascular Research and Clinical Trials, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA.

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